ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.4157+105A>G

dbSNP: rs550251651
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001593743 SCV001816883 likely benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001593743 SCV005223957 likely benign not provided criteria provided, single submitter not provided

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